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Hyperlysinemia, saccharopinuria, and 2-aminoadipic and 2-oxoadipic aciduria are generally considered benign disorders [27,34]: Glutaric aciduria type 1 is a rare autosomal recessive disease caused by glutaryl-CoA dehydrogenase deficiency
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3.2 Treatment outcome Ten out of fifteen patients (67%) completed the 16-week trial
